HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88007786_88007787delinsCG , CM000666.2:g.88007786_88007787delinsCG | GRCh38 |
NC_000004.11:g.88928938_88928939delinsCG , CM000666.1:g.88928938_88928939delinsCG | GRCh37 |
NC_000004.10:g.89147962_89147963delinsCG | NCBI36 |
NG_008604.1:g.5119_5120delinsCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.53_54delinsCG MANE Select | ENSP00000237596.2:p.Pro18= | |
ENST00000237596.6:c.53_54delinsCG | ENSP00000237596.2:p.Pro18= | |
NM_000297.3:c.53_54delinsCG | NP_000288.1:p.Pro18= | |
XM_011532028.1:c.53_54delinsCG | XP_011530330.1:p.Pro18= | |
XR_244632.2:n.148_149delinsCG | ||
NR_156488.1:n.140_141delinsCG | ||
XM_011532028.2:c.53_54delinsCG | XP_011530330.1:p.Pro18= | |
NM_000297.4:c.53_54delinsCG MANE Select | NP_000288.1:p.Pro18= | |
NR_156488.2:n.152_153delinsCG |